A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250607



Internal ID21306193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33186351..33207997hg38UCSC Ensembl
Outerchr14:33182689..33209038hg38UCSC Ensembl
Innerchr14:33655557..33677203hg19UCSC Ensembl
Outerchr14:33651895..33678244hg19UCSC Ensembl
Innerchr14:32725308..32746954hg18UCSC Ensembl
Outerchr14:32721646..32747995hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3826350
hg1926350
hg1826350
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169419
Supporting Variants
SamplesNGO_26
Known GenesNPAS3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250607
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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